Effect of PLA crystallization on the structure of biomimetic composites of PLA and clay

Composites of poly(lactic acid) (PLA) and organoclays with clay loadings of up to 80% were prepared as self‐supporting films using a doctor‐blading approach. Depending on the properties of the used organoclay, either intercalated nanocomposites or conventional composites were obtained. The incorporation of such high amounts of clay resulted in up to 10‐fold decrease in the water vapor transmission rate when compared to the pristine polymer. The effect of clay platelets on the crystallization of PLA chains was also studied; it was found that high amounts of clay hinder only the melt crystallization of the polymer, whereas cold crystallization proceeds as usual. On the other hand, the crystallization of PLA also influenced the composite structure by increasing the extent of intercalation of polymer between clay layers. This study thus shows that the change in the extent of clay‐polymer interactions is also an important factor in controlling nanocomposite structure, especially for high loading. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Linear viscoelastic behavior of compatibilized PMMA/PP blends

In this work, the morphology and linear viscoelastic behavior of PMMA/PP blends to which a graft copolymer PP‐g‐PMMA has been added was studied. The copolymer concentration varied from 1 to 10 wt % relative to the dispersed phase concentration. The rheological data were used to infer the interfacial tension between the blended components. It was observed that PP‐g‐PMMA was effective as a compatibilizer for PMMA/PP blends. For PP‐g‐PMMA concentration added below the critical concentration of interface saturation, two rheological behaviors were observed depending on the blend concentration: for 70/30 blend, the storage modulus, at low frequencies, increased as compared to the one of the unmodified blend; for 90/10 blend, it decreased. For 90/10 blend, the relaxation spectrum presented an interfacial relaxation time related to the presence of the compatibilizer (τ_β). For PP‐g‐PMMA concentrations added above the critical concentration of interface saturation, the storage modulus of all blends increased as compared with the one of the unmodified blend. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Edge Chipping Resistance of Alumina/Zirconia Laminates

The edge chipping test was used to measure the fracture resistance of alumina/alumina‐zirconia laminated structures. Tailored, symmetrical laminated structures were prepared with a variety of layer thickness. The laminates had a significantly greater edge chipping resistance. Laminates with thin layers were just as effective in impeding edge chips as laminates with thick layers.     

Chemical Analysis with High Spatial Resolution by Rutherford Backscattering and Raman Confocal Spectroscopies: Surface Hierarchically Structured Glasses

Copper and iron in glasses constitute classical aims of study because of the optical effects that they produce. Structured materials are also interesting due to the incorporated functionalities derived from their spatial organization. Here, CuO and Fe₂O₃ were incorporated into a standard glass, from which glass coatings with different thicknesses were studied. Whereas iron cations dissolved in the glassy matrix, copper cations saturated it and crystallized at the surface, forming a hierarchical microstructure. The surface microstructure consisted of crystallizations of Tenorite (CuO) forming interconnected walls. The walls surrounding areas of glassy matrix gave rise to a cells microstructure. Rutherford Backscattering Spectrometry provided the composition of the samples with high depth resolution, and Raman Confocal Microscopy determined the phases location and their distribution forming the microstructure. The joint information from both techniques allowed high chemical and spatial resolution of the main cations location for the hierarchical surface microstructure.     

Effects of chemical and thermochemical pretreatments on sunflower oil cake in biochemical methane potential assays

BACKGROUND: The effects of chemical and thermochemical pretreatments on the composition and anaerobic biodegradability of sunflower oil cake were studied to compare these pretreatments and to assess their effectiveness. Four reagents (lime, sodium hydroxide, sulphuric acid, and sodium bicarbonate) at concentrations of 25% (w/w) of dry weight of substrate and 20 g L^?1 substrate concentration were used for the chemical pretreatment for 4 h. The same conditions were used for thermochemical pretreatment with heating at 75°C. After the pretreatments, the solid and liquid fractions were separated and subjected to biochemical methane potential tests. RESULTS: The methane yields of the solid fraction obtained with lime, sodium hydroxide, sulphuric acid and bicarbonate were 130±9, 54±4, 61±6 and 88±7 mL CH₄ g^‐1COD_added, respectively, and after thermochemical pretreatment were 26±2, 84±7, 74±7, and 77±6 mL CH₄ g^‐1COD_added, respectively. The methane yields for liquids were 152±13, 2±0, 0±0, 249±19 mL CH₄ g^‐1COD_added, for the chemical pre‐treatment, respectively, and after the thermochemical pretreatment were 273±13, 58±5, 0±0 and 145±12 mL CH₄ g^‐1COD_added, respectively. CONCLUSION: Only the solid fraction obtained after the chemical pretreatment with lime gave a methane yield higher (130 mL CH₄ g^‐1COD_added) than the obtained for the untreated solid material (114 mL CH₄ g^‐1COD_add). No thermochemical pretreatment enhanced the methane yield of the solid or liquid fractions of the untreated material. © 2012 Society of Chemical Industry     

Modification of Polycarbonate and Glycol Modified Poly(ethylene terephthalate) by Addition of Silica‐Nanoparticles Grafted with SAN Copolymer Using “Classical” and ARGET ATRP

This study presents a nanocomposite manufacturing route starting from non‐functionalized nanosilica and SAN surface modification via “grafting from” ATRP up to processing of transparent polycarbonate and glycol modified poly(ethylene terephthalate) nanocomposites. Synthesis limitations of low molecular weight graft SAN derived from “classical” ATRP are overcome by employment of the emerging ARGET ATRP. Mechanical investigations of polycarbonate and glycol modified poly(ethylene terephthalate) nanocomposites present up to 80% enhancement of creep performance and additionally 70% enhancement against wear abrasion for glycol modified poly(ethylene terephthalate) nanocomposites. Strength and tensile modulus are only moderately influenced by the addition of nanoparticles. Morphological studies confirm that the present modification route is able to create uniform dispersions of single particles and small particle aggregates in polymer matrices.

     

Mode II Fracture Toughness of a Brittle and a Ductile Adhesive as a Function of the Adhesive Thickness

The main goal of this study was to evaluate the effect of the thickness and type of adhesive on the Mode II toughness of an adhesive joint. Two different adhesives were used, Araldite ® AV138/HV998 which is brittle and Araldite 2015 which is ductile. The end notched flexure (ENF) test was used to determine the Mode II fracture toughness because it is commonly known to be the easiest and widely used to characterize Mode II fracture. The ENF test consists of a three-point bending test on a notched specimen which induces a shear crack propagation through the bondline. The main conclusion is that the energy release rate for AV138 does not vary with the adhesive thickness whereas for Araldite 2015, the fracture toughness in Mode II increases with the adhesive thickness. This can be explained by the adhesive plasticity at the end of the crack tip.     

Preparation of chitosan‐based adhesives and assessment of their mechanical properties

The aim of this study is to develop chitosan‐based adhesives and to characterize their shear strength. The desirable features of such adhesives are biodegradability, biocompatibility, non‐toxicity, and anti‐microbial properties. Various eco‐friendly polyanionic polysaccharides, acids, and plasticizers, in single or multiple formulations, were associated with chitosan. The resulting crosslinked polymers were glued on some chemically treated aluminum adherends. The shear strength of these formulations was measured with the “double lap‐joint” bonding method, as it features a low‐peeling effect. The shear strength of 40.8 MPa obtained for formulations containing chitosan and glycerol plasticizer was the most significant finding in this study. This value is equivalent to that obtained with a synthetic adhesive used in industry. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Relation between Electrical Mobility,Mass, and Size for Nanodrops 1–6.5 nm in Diameter in Air

A large number of data on mobility and mass have been newly obtained or reanalyzed for clusters of a diversity of materials, with the aim of determining the relation between electrical mobility (Z) and mass diameter d _m = (6m/ π ρ ) ^1/3 (m is the particle mass and ρ the bulk density of the material forming the cluster) for nanoparticles with d _m ranging from 1 nm to 6.5 nm. The clusters were generated by electrospraying solutions of ionic liquids, tetra-alkyl ammonium salts, cyclodextrin, bradykinin, etc., in acetonitrile, ethanol, water, or formamide. Their electrical mobilities Z in air were measured directly by a differential mobility analyzer (DMA) of high resolution. Their masses m were determined either directly via mass spectrometry, or assigned indirectly by first distinguishing singly (z = 1) and doubly (z = 2) charged clusters, and then identifying monomers, dimers, … n-mers, etc., from their ordering in the mobility spectrum. Provided that d _m > 1.3 nm, data of the form d _m vs. [z(1+m _g /m) ^1/2 /Z)] ^1/2 fall in a single curve for nanodrops of ionic liquids (ILs) for which ρ is known (m _g is the mass of the molecules of suspending gas). Using an effective particle diameter d _p = d _m + d _g and a gas molecule diameter d _g = 0.300 nm, this curve is also in excellent agreement with the Stokes-Millikan law for spheres. Particles of solid materials fit similarly well the same Stokes-Millikan law when their (unknown) bulk density is assigned appropriately.